Akkari PA - Search Results

1

Targeted Molecular Therapeutics for Parkinson's Disease: A Role for Antisense Oligonucleotides?

Li D, Mastaglia FL, Yau WY, Chen S, Wilton SD, Akkari PA. Li D, et al. Among authors: akkari pa. Mov Disord. 2022 Nov;37(11):2184-2190. doi: 10.1002/mds.29201. Epub 2022 Aug 29. Mov Disord. 2022. PMID: 36036206 Free PMC article. No abstract available.

2

Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation.

Hunt CC, Eyre HJ, Akkari PA, Meredith C, Dorosz SM, Wilton SD, Callen DF, Laing NG, Baker E. Hunt CC, et al. Among authors: akkari pa. Cytogenet Cell Genet. 1995;71(1):94-5. doi: 10.1159/000134070. Cytogenet Cell Genet. 1995. PMID: 7606936

3

A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy.

Laing NG, Wilton SD, Akkari PA, Dorosz S, Boundy K, Kneebone C, Blumbergs P, White S, Watkins H, Love DR, et al. Laing NG, et al. Among authors: akkari pa. Nat Genet. 1995 Jan;9(1):75-9. doi: 10.1038/ng0195-75. Nat Genet. 1995. PMID: 7704029

4

Assignment of the human skeletal muscle alpha-tropomyosin gene (TPM1) to band 15q22 by fluorescence in situ hybridization.

Eyre H, Akkari PA, Wilton SD, Callen DC, Baker E, Laing NG. Eyre H, et al. Among authors: akkari pa. Cytogenet Cell Genet. 1995;69(1-2):15-7. doi: 10.1159/000133928. Cytogenet Cell Genet. 1995. PMID: 7835079

5

Assignment of the human a-tropomyosin gene TPM3 to 1q22-->q23 by fluorescence in situ hybridisation.

Wilton SD, Eyre H, Akkari PA, Watkins HC, MacRae C, Laing NG, Callen DC. Wilton SD, et al. Among authors: akkari pa. Cytogenet Cell Genet. 1995;68(1-2):122-4. doi: 10.1159/000133905. Cytogenet Cell Genet. 1995. PMID: 7956350

6

Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation.

Akkari PA, Eyre HJ, Wilton SD, Callen DF, Lane SA, Meredith C, Kedes L, Laing NG. Akkari PA, et al. Cytogenet Cell Genet. 1994;65(4):265-7. doi: 10.1159/000133644. Cytogenet Cell Genet. 1994. PMID: 8258301

7

Assignment of the human slow skeletal muscle troponin gene (TNNI1) to 1q32 by fluorescence in situ hybridisation.

Eyre HJ, Akkari PA, Meredith C, Wilton SD, Callen DC, Kedes L, Laing NG. Eyre HJ, et al. Among authors: akkari pa. Cytogenet Cell Genet. 1993;62(2-3):181-2. doi: 10.1159/000133467. Cytogenet Cell Genet. 1993. PMID: 8428521

8

A splice-site mutation causing ovine McArdle's disease.

Tan P, Allen JG, Wilton SD, Akkari PA, Huxtable CR, Laing NG. Tan P, et al. Among authors: akkari pa. Neuromuscul Disord. 1997 Jul;7(5):336-42. doi: 10.1016/s0960-8966(97)00062-x. Neuromuscul Disord. 1997. PMID: 9267848

9

Early onset chromosome 14-linked distal myopathy (Laing).

Mastaglia FL, Phillips BA, Cala LA, Meredith C, Egli S, Akkari PA, Laing NG. Mastaglia FL, et al. Among authors: akkari pa. Neuromuscul Disord. 2002 May;12(4):350-7. doi: 10.1016/s0960-8966(01)00287-5. Neuromuscul Disord. 2002. PMID: 12062252

10

Altered Gut Microbiome in Parkinson's Disease and the Influence of Lipopolysaccharide in a Human α-Synuclein Over-Expressing Mouse Model.

Gorecki AM, Preskey L, Bakeberg MC, Kenna JE, Gildenhuys C, MacDougall G, Dunlop SA, Mastaglia FL, Akkari PA, Koengten F, Anderton RS. Gorecki AM, et al. Among authors: akkari pa. Front Neurosci. 2019 Aug 7;13:839. doi: 10.3389/fnins.2019.00839. eCollection 2019. Front Neurosci. 2019. PMID: 31440136 Free PMC article.

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